首页> 美国卫生研究院文献>Journal of Bacteriology >Characterization of a gene involved in histidine biosynthesis in Halobacterium (Haloferax) volcanii: isolation and rapid mapping by transformation of an auxotroph with cosmid DNA.
【2h】

Characterization of a gene involved in histidine biosynthesis in Halobacterium (Haloferax) volcanii: isolation and rapid mapping by transformation of an auxotroph with cosmid DNA.

机译:火山嗜盐杆菌(Haloferax)中参与组氨酸生物合成的基因的表征:通过用粘粒DNA转化营养缺陷型进行分离和快速定位。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Techniques for the transformation of halophilic archaebacteria have been developed recently and hold much promise for the characterization of these organisms at the molecular level. In order to understand genome organization and gene regulation in halobacteria, we have begun the characterization of genes involved in amino acid biosynthesis in Halobacterium (Haloferax) volcanii. These studies are facilitated by the many auxotrophic mutants of H. volcanii that have been isolated. In this project we demonstrate that cosmid DNA prepared from Escherichia coli can be used to transform an H. volcanii histidine auxotroph to prototrophy. A set of cosmid clones covering most of the genome of H. volcanii was used to isolate the gene which is defective in H. volcanii WR256. Subcloning identified a 1.6-kilobase region responsible for transformation. DNA sequence analysis of this region revealed an open reading frame encoding a putative protein 361 amino acids in length. A search of the DNA and protein data bases revealed that this open reading frame encodes histidinol-phosphate aminotransferase (EC 2.6.1.9), the sequence of which is also known for E. coli, Bacillus subtilis, and Saccharomyces cerevisiae.
机译:最近已经开发了用于转化嗜盐古细菌的技术,并在分子水平上表征这些生物具有广阔的前景。为了了解盐杆菌中的基因组组织和基因调控,我们已经开始鉴定参与火山盐杆菌(Haloferax)的氨基酸生物合成的基因。这些研究得到了已经分离的许多H. volcanii营养缺陷型突变体的帮助。在这个项目中,我们证明了从大肠杆菌制备的粘粒DNA可用于将火山嗜血杆菌组氨酸营养缺陷型转化为原养型。一组覆盖火山嗜血菌大部分基因组的粘粒克隆被用于分离在火山嗜血菌WR256中有缺陷的基因。亚克隆鉴定出负责转化的1.6碱基对区域。该区域的DNA序列分析揭示了一个开放阅读框,其编码假定的361个氨基酸。对DNA和蛋白质数据库的搜索显示,该开放阅读框编码组氨醇磷酸氨基转移酶(EC 2.6.1.9),大肠杆菌,枯草芽孢杆菌和酿酒酵母也已知该序列。

著录项

相似文献

  • 外文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号